Anatomic Distribution and Clinical Presentation of Pulmonary Carcinoids: A Single-institutional Study.

Publication/Presentation Date

6-1-2025

Abstract

BACKGROUND: Pulmonary carcinoid tumors (PCTs) have historically manifested predominantly as central lung lesions causing postobstructive symptoms. However, nearly all case series of PCTs to date evaluate cohorts in years before 2010. Because an increased volume of cross-sectional imaging studies results in more frequent detection of incidental lung nodules, we sought to evaluate whether the nature of this cancer's clinical characteristics may be evolving by studying a contemporary series of patients.

METHODS: The study analyzed all patients with a diagnosis of PCT at Thomas Jefferson University Hospital (Philadelphia, PA) between 2006 and 2020. The study evaluated tumor location within the bronchial tree (ie, central or peripheral), the presence or absence of symptoms at diagnosis, patient demographics, and nodule characteristics on computed tomography.

RESULTS: A total of 73 PCTs were analyzed in 72 patients. Most PCTs were detected incidentally (48 of 72; 95% CI: 55%-77%) and located peripherally (41 of 67; 95% CI: 49%-73%). Logistic regression analysis demonstrated that the likelihood of PCTs having these features increased over the study period.

CONCLUSIONS: PCTs manifested predominantly as peripheral lung lesions detected incidentally on computed tomography, which contrasts with the existing literature. This may reflect the changing nature of PCT diagnosis as cross-sectional imaging volume has increased. Clinicians should be mindful that incidental solitary pulmonary nodules detected on chest imaging may represent PCT, especially if the lesions are slow growing.

Volume

3

Issue

2

First Page

299

Last Page

303

ISSN

2772-9931

Disciplines

Business Administration, Management, and Operations | Health and Medical Administration | Management Sciences and Quantitative Methods

PubMedID

40525197

Department(s)

Administration and Leadership

Document Type

Article

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